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The dynamic effect of genetic variation on the in vivo ER stress transcriptional response in different tissues

The genetic regulation of gene expression varies greatly across tissue-type and individuals and can be strongly influenced by the environment. Many variants, under healthy control conditions, may be silent or even have the opposite effect under diseased stress conditions. This study uses an in vivo...

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Autores principales: Russell, Nikki D, Chow, Clement Y
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157157/
https://www.ncbi.nlm.nih.gov/pubmed/35485945
http://dx.doi.org/10.1093/g3journal/jkac104
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author Russell, Nikki D
Chow, Clement Y
author_facet Russell, Nikki D
Chow, Clement Y
author_sort Russell, Nikki D
collection PubMed
description The genetic regulation of gene expression varies greatly across tissue-type and individuals and can be strongly influenced by the environment. Many variants, under healthy control conditions, may be silent or even have the opposite effect under diseased stress conditions. This study uses an in vivo mouse model to investigate how the effect of genetic variation changes with cellular stress across different tissues. Endoplasmic reticulum stress occurs when misfolded proteins accumulate in the endoplasmic reticulum. This triggers the unfolded protein response, a large transcriptional response which attempts to restore homeostasis. This transcriptional response, despite being a conserved, basic cellular process, is highly variable across different genetic backgrounds, making it an ideal system to study the dynamic effects of genetic variation. In this study, we sought to better understand how genetic variation alters expression across tissues, in the presence and absence of endoplasmic reticulum stress. The use of different mouse strains and their F1s allow us to also identify context-specific cis- and trans- regulatory variation underlying variable transcriptional responses. We found hundreds of genes that respond to endoplasmic reticulum stress in a tissue- and/or genotype-dependent manner. The majority of the regulatory effects we identified were acting in cis-, which in turn, contribute to the variable endoplasmic reticulum stress- and tissue-specific transcriptional response. This study demonstrates the need for incorporating environmental stressors across multiple different tissues in future studies to better elucidate the effect of any particular genetic factor in basic biological pathways, like the endoplasmic reticulum stress response.
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spelling pubmed-91571572022-06-04 The dynamic effect of genetic variation on the in vivo ER stress transcriptional response in different tissues Russell, Nikki D Chow, Clement Y G3 (Bethesda) Investigation The genetic regulation of gene expression varies greatly across tissue-type and individuals and can be strongly influenced by the environment. Many variants, under healthy control conditions, may be silent or even have the opposite effect under diseased stress conditions. This study uses an in vivo mouse model to investigate how the effect of genetic variation changes with cellular stress across different tissues. Endoplasmic reticulum stress occurs when misfolded proteins accumulate in the endoplasmic reticulum. This triggers the unfolded protein response, a large transcriptional response which attempts to restore homeostasis. This transcriptional response, despite being a conserved, basic cellular process, is highly variable across different genetic backgrounds, making it an ideal system to study the dynamic effects of genetic variation. In this study, we sought to better understand how genetic variation alters expression across tissues, in the presence and absence of endoplasmic reticulum stress. The use of different mouse strains and their F1s allow us to also identify context-specific cis- and trans- regulatory variation underlying variable transcriptional responses. We found hundreds of genes that respond to endoplasmic reticulum stress in a tissue- and/or genotype-dependent manner. The majority of the regulatory effects we identified were acting in cis-, which in turn, contribute to the variable endoplasmic reticulum stress- and tissue-specific transcriptional response. This study demonstrates the need for incorporating environmental stressors across multiple different tissues in future studies to better elucidate the effect of any particular genetic factor in basic biological pathways, like the endoplasmic reticulum stress response. Oxford University Press 2022-04-29 /pmc/articles/PMC9157157/ /pubmed/35485945 http://dx.doi.org/10.1093/g3journal/jkac104 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
Russell, Nikki D
Chow, Clement Y
The dynamic effect of genetic variation on the in vivo ER stress transcriptional response in different tissues
title The dynamic effect of genetic variation on the in vivo ER stress transcriptional response in different tissues
title_full The dynamic effect of genetic variation on the in vivo ER stress transcriptional response in different tissues
title_fullStr The dynamic effect of genetic variation on the in vivo ER stress transcriptional response in different tissues
title_full_unstemmed The dynamic effect of genetic variation on the in vivo ER stress transcriptional response in different tissues
title_short The dynamic effect of genetic variation on the in vivo ER stress transcriptional response in different tissues
title_sort dynamic effect of genetic variation on the in vivo er stress transcriptional response in different tissues
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157157/
https://www.ncbi.nlm.nih.gov/pubmed/35485945
http://dx.doi.org/10.1093/g3journal/jkac104
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